Analysis of Sport Specific Adaptations of the Shoulder in Adolescent Elite Handball Players and the Influence of the Preventive Use of Tape on These Outcome Measurements.

June 22, 2011 updated by: University Ghent

Analysis of Sport Specific Adaptations of the Shoulder in Adolescent Elite Handball Players and the Influence of the Preventive Use of Tape on Shoulder Strength, Mobility, the Position of the Scapula and the Size of the Subacromial Space.

Shoulder complaints are very common in overhead athletes.The application of kinesiotape that keeps the shoulder in a correct position is used to avoid this.

This could enlarge the dynamic size of the subacromial space and thus contribute to prevention of shoulder injuries.

30 young elite handball players will participate in this study.Researchers will perform a number of measurements before and after applying kinesiotape to correct shoulder position:

  • measurement of subacromial space
  • measurement of 3D kinematics of shoulder
  • assessment of shoulder posture

Hypothesis of this study is that tape can influence the position of the scapula and is therefore able to change the size of the subacromial space.This results in a more efficient use of shoulder muscles with higher maximal strength as a result and maximizes shoulder mobility.

Study Overview

Detailed Description

Shoulder complaints are very common in overhead athletes. Throwing motions question large explosive strength and stability of the intrinsic instable shoulder joint. Malpositioning of the scapula increases the risk of overload injuries.

The application of kinesiotape that keeps the shoulder in a correct position is used to avoid this. Until now no studies have shown if the tape is able to correct the position of the scapula. If this is the case, the application of the tape could enlarge the dynamic size of the subacromial space (virtual space in the shoulder in which rotator cuff tendons run through) and thus contribute to prevention of shoulder injuries.

This study will take place in collaboration with Prof. Dr. Robert Van Cingel, director of the Sports Medical Center Papendal(SMCP) in the Netherlands. SMCP is a multidisciplinary center for sports medicine, sports rehabilitation and sports cardiology.

30 young elite handball players will participate in this study. Three researchers will perform a number of measurements before and after applying kinesiotape to correct shoulder position.

  1. Measurement of the size of the subacromial space with dynamic ultrasound. Ultrasound is completely harmless and painless.
  2. Measurement of three-dimensional kinematics of the shoulder with FASTRAK. Sensors are placed on the skin of the shoulder with adhesive tape. Both placement of markers and measurements are non-invasive and painless.
  3. Assessment of shoulder posture by measuring several angles and distances. Measurement of shoulder strength and mobility. These measurements are all non-invasive and painless.

Hypothesis of this study is that tape can influence the position of the scapula and is therefore able to change the size of the subacromial space. This results in a more efficient use of shoulder muscles with higher maximal strength as a result and maximizes shoulder mobility.

Study Type

Interventional

Enrollment (Anticipated)

30

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Arnhem, Netherlands
        • Sports Medical Center of Papendal

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

15 years to 25 years (Child, Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

Female

Description

Inclusion Criteria:

  • Elite handball players of Papendal
  • age between 15 and 25
  • more than 15 hours of handball training/week
  • female

Exclusion Criteria:

  • shoulder pain at the moment for which a doctor was consulted

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Kinesiotape
Kinesiotape will be applied to the correct shoulder position of the participants.
Measurement of the size of the subacromial space with dynamic ultrasound.
Measurements of the 3D-kinematics of the shoulder with FASTRAK. Sensors are placed on the skin of the shoulder with adhesive tape.
Assessment of shoulder posture by measuring several angles and distances.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
effect of kinesiotape
Time Frame: 2 days
Immediate effects of applying kinesiotape to the correct shoulder position
2 days

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Ann Cools, Ph.D., University Ghent

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

November 1, 2010

Primary Completion (Actual)

November 1, 2010

Study Completion (Actual)

November 1, 2010

Study Registration Dates

First Submitted

December 14, 2010

First Submitted That Met QC Criteria

December 22, 2010

First Posted (Estimate)

December 24, 2010

Study Record Updates

Last Update Posted (Estimate)

June 23, 2011

Last Update Submitted That Met QC Criteria

June 22, 2011

Last Verified

June 1, 2011

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • EC/2010/637

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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